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A study on the kinetics of syngas production from glycerol over alumina-supported samarium-nickel catalyst

机译:氧化铝负载sa镍催化剂上甘油制合成气动力学研究

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摘要

The current paper reports on the kinetics of syngas production from glycerol pyrolysis over the alumina-supported nickel catalyst that was promoted with samarium, a rare earth element. The catalysts were synthesized via wet-impregnation method and its physicochemical properties were subsequently characterized. Reaction studies were performed in a 10 mm-ID stainless steel fixed bed reactor with reaction temperatures maintained at 973, 1023 and 1073 K, respectively, employing weight-hourly-space-velocity of 4.5 x 10(4) ml g(-1) h(-1). The textural property examination showed that BET specific surface area was 2.09 m(2) for the unpromoted catalyst while the samarium promoted catalyst has 2.68 m(2) g(-1). Interestingly, the results were supported by the FESEM images which showed that the promoted catalyst has smaller particle size compared to the unpromoted catalyst. Furthermore, the NH3- and CO2-TPD analyses proved that the strong and weak acid-basic sites were present. During glycerol pyrolysis, the syngas was produced directly from the glycerol decomposition. This has created H-2:CO ratios that were always lower than 2.0, which is suitable for Fischer-Tropsch synthesis. The activation energy based on power law modeling for the unpromoted catalyst was 35.8 kJ mol(-1) and 23.4 kJ mol(-1) for Sm-promoted catalyst with reaction order 1.20 and 1.10, respectively. Experimental data were also fitted to the Langmuir-Hinshelwood model. Upon subjected to both statistical and thermodynamics consistency criteria, it can be conclusively proved that single-site mechanisms with associative adsorption of glycerol best describe the glycerol pyrolysis over both unpromoted and Sm promoted catalyst in the current work, with regression coefficient values of more than 0.9. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:本论文报道了在稀土元素sa促进的氧化铝负载的镍催化剂上甘油热解制合成气的动力学。通过湿浸渍法合成了催化剂,并对其理化性质进行了表征。反应研究是在10 mm ID的不锈钢固定床反应器中进行的,反应温度分别保持在973、1023和1073 K,采用的时空速度为4.5 x 10(4)ml g(-1) h(-1)。织构性能检查表明,对于未助催化剂,BET比表面积为2.09 m(2),而promote助催化剂为2.68 m(2)g(-1)。有趣的是,该结果得到了FESEM图像的支持,该图像表明与未助催化剂相比,助催化剂的粒径较小。此外,NH3-和CO2-TPD分析证明存在强酸和弱酸碱性位点。在甘油热解过程中,合成气直接由甘油分解产生。这样产生的H-2:CO比率始终低于2.0,非常适合费-托合成。基于幂律模型的未助催化剂的活化能分别为Sm助催化剂的35.8 kJ mol(-1)和23.4 kJ mol(-1),反应级分别为1.20和1.10。实验数据也适用于Langmuir-Hinshelwood模型。根据统计和热力学一致性标准,可以得出结论,单点机理与甘油的联合吸附最能描述当前工作中未助催化和Sm助催化的甘油热解,回归系数值大于0.9 。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2016年第25期|10568-10577|共10页
  • 作者单位

    Univ Malaysia Pahang, Fac Chem & Nat Resources Engn, Gambang 26300, Pahang, Malaysia;

    Univ Malaysia Pahang, Fac Chem & Nat Resources Engn, Gambang 26300, Pahang, Malaysia|Univ Malaysia Pahang, Ctr Excellence Adv Res Fluid Flow CARIFF, Gambang 26300, Pahang, Malaysia;

    Univ Malaysia Pahang, Fac Chem & Nat Resources Engn, Gambang 26300, Pahang, Malaysia|Univ Malaysia Pahang, Ctr Excellence Adv Res Fluid Flow CARIFF, Gambang 26300, Pahang, Malaysia;

    Univ New South Wales, Sch Chem Engn, Sydney, NSW 2052, Australia;

    Univ Malaysia Pahang, Fac Chem & Nat Resources Engn, Gambang 26300, Pahang, Malaysia|Univ Malaysia Pahang, Ctr Excellence Adv Res Fluid Flow CARIFF, Gambang 26300, Pahang, Malaysia|Univ Malaysia Pahang, Rare Earth Res Ctr RERC, Gambang 26300, Pahang, Malaysia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Glycerol; Pyrolysis; Nickel; Samarium; Kinetics; Syngas;

    机译:甘油;热解;镍;Sa;运动学;合成气;
  • 入库时间 2022-08-18 00:20:16

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